The objective of our study was to evaluate reparative tissues formed in cho
ndral defects in an adult canine model implanted with cultured autologous a
rticular chondrocytes seeded in type I and LI collagen-GAG matrices. Two de
fects were produced in the trochlea grooves of the knees of 21 dogs, with c
artilage removed down to the tidemark. This study includes the evaluation o
f 36 defects distributed among five treatment groups: Group A, type II coll
agen matrix seeded with autologous chondrocytes under a sutured type II col
lagen flap; Group B, type I collagen matrices seeded with chondrocytes unde
r a sutured fascia flap; Group C, unseeded type I collagen matrix implanted
under a sutured fascia flap; Group D, fascia lata flap alone; and Group E,
untreated defects. All animals were killed 15 weeks after implantation. Si
x other defects were created at the time of death and evaluated immediately
after production as 'acute defect controls'. In three additional defects,
unseeded matrices were sutured to the defect and the knee closed and reopen
ed after 30 min to determine if early displacement of the graft was occurri
ng; these defects served as 'acute implant controls'. The areal percentages
of four tissue types in the chondral zone of the original defect were dete
rmined histomorphometrically: fibrous tissue (FT); hyaline cartilage (HC);
transitional tissue (TT, including fibrocartilage); and articular cartilage
(AC). New tissue formed in the remodeling subchondral bone underlying cert
ain defects was also assessed. Bonding of the repair tissue to the subchond
ral plate and adjacent cartilage, and degradation of the adjacent tissues w
ere evaluated.
There were no significant differences in the tissues filling the original d
efect area of the sites treated with chondrocyte-seeded type I and type II
matrices. Most of the tissue in the area of the original defect in all of t
he groups was FT and TT. The areal percentage of HC plus AC was highest in
group E, with little such tissue in the cell-seeded groups, and none in gro
ups C and D. The greatest total amount of reparative tissue, however, was f
ound in the cell-seeded type II matrix group. Moreover, examination of the
reparative tissue formed in the subchondral region of defects treated with
the chondrocyte-seeded collagen matrices (Groups A and B) demonstrated that
the majority of the tissue was positive for type II collagen and stained w
ith safranin O. These results indicate an influence of the exogenous chondr
ocytes on the process of chondrogenesis in this site. In all groups with im
plants (A-D), 30-50% of the FT and TT was bonded to the adjacent cartilage.
Little of this tissue (6-22%) was attached to the subchondral plate, which
was only about 50% intact. Remarkable suture damage was found in sections
from each group in which sutures were used. Harvest sites showed no regener
ation of normal articular cartilage, 18 weeks after the biopsy procedure.
Future studies need to investigate other matrix characteristics, and the ef
fects of cell density and incubation of the seeded sponges prior to implant
ation on the regenerative response. (C) 1998 Elsevier Science Ltd. All righ
ts reserved.